4.6 Review Book Chapter

Mitochondrial Complex I

Journal

ANNUAL REVIEW OF BIOCHEMISTRY, VOL 82
Volume 82, Issue -, Pages 551-575

Publisher

ANNUAL REVIEWS
DOI: 10.1146/annurev-biochem-070511-103700

Keywords

complex I dysfunction; electron transfer; electron transport chain; NADH:ubiquinone oxidoreductase; proton transfer; superoxide production

Funding

  1. Medical Research Council [MC_U105663141] Funding Source: Medline
  2. MRC [MC_U105663141] Funding Source: UKRI

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Complex I (NADH: ubiquinone oxidoreductase) is crucial for respiration in many aerobic organisms. In mitochondria, it oxidizes NADH from the tricarboxylic acid cycle and beta-oxidation, reduces ubiquinone, and transports protons across the inner membrane, contributing to the proton-motive force. It is also a major contributor to cellular production of reactive oxygen species. The redox reaction of complex I is catalyzed in the hydrophilic domain; it comprises NADH oxidation by a flavin mononucleotide, intramolecular electron transfer along a chain of iron-sulfur clusters, and ubiquinone reduction. Redox-coupled proton translocation in the membrane domain requires long-range energy transfer through the protein complex, and the molecular mechanisms that couple the redox and proton-transfer half-reactions are currently unknown. This review evaluates extant data on the mechanisms of energy transduction and superoxide production by complex I, discusses contemporary mechanistic models, and explores how mechanistic studies may contribute to understanding the roles of complex I dysfunctions in human diseases.

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